Variant #0000344644 (NC_000009.11:g.131388081C>G, NM_001130438.2:c.6103C>G (SPTAN1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.131388081C>G
DNA change (hg38) g.128625802C>G
Published as SPTAN1(NM_001130438.2):c.6103C>G (p.(Gln2035Glu))
ISCN -
DB-ID SPTAN1_000066 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTAN1 NM_001130438.2 ?/. - c.6103C>G r.(?) p.(Gln2035Glu)
WDR34 NM_052844.3 ?/. - c.*7942G>C r.(=) p.(=)


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